On this very cold, sub-zero, day I’m very blessed and pleased the specialist in Boston didn’t want to see me this week. Only the second week since coming home from ending a month’s stay there in early July that we haven’t had the tiring nearly 500 mile round trip there and back.

Next visit on November 14th.

The thrush in my mouth and throat is still present and sore – but I do feel somewhat more energetic and motivated most days.

Hoping the US election result will cause all parties to work together in a united way and get the country governed better.

Hope Lodge, Wednesday , October 31st 2012

“Rejoice and be exceedingly glad”. Matthew, 5:12.

We are rejoicing and are exceedingly glad… for the way the Lord looks after the details. I discover today that the bookings I had made to stay at the Hope Lodge through to the end of the year were not quite as I had thought. I had thought I had asked for a room every week but for some reason the lady who looks after the bookings had made them from the start of October for every 2 weeks… so the weeks Noel’s sister and brother were visiting and Toby drove us to Boston and home in one day, we actually did not have bookings! Kate said she was confused by the voice mails I had left canceling the room for those weeks… as we did not have one anyway! And since Dr. Soiffer today told Noel to take next week off we don’t need one next week… good thing as it was not booked! Now the prayer, please, is that Noel will stay well and will be on 2 weekly appointments from now on… as otherwise there is no room in the Inn and we will have to pay for a hotel room as the lodge is fully booked to the end of the year. Praise God for being in the detail.

Hurricane Sandy blew through our area on Monday night but we were spared any lasting damage for which we are thankful: but our hearts and prayers go out to the many, many people who have suffered devastating losses and long term damage. The only slight effect it had on our family was to extend JoAnn’s little vacation by a day. On Monday, when she and her sisters arrived back from their cruise, JoAnn and Melanie’s flight to Albany was cancelled although Judy did get home to Kansas. Lucy took the news of Mommy not getting home as expected for a 2 year old – in her stride, being quite happy being in the company of those who love her. For Charlotte it was more difficult, as you would expect from a 5 year old. She was upset but showed great courage and strength of character and was able to put her disappointment aside and be her normal cheerful self… thankfully fights to Albany resumed on Tuesday and JoAnn got home safely then.

This past week Noel has been regaining some strength and eating more even put on some of the weight he had lost, although he still has the sore mouth and upset digestive system… he is coping OK with it. We were looking forward to encouraging news this week from his tests and at his appointments today we were encouraged as his blood and liver function levels were not any worse but had stayed very much the same as last week. Dr. Soiffer took this a good sign, so said he would leave all his medications at the same level but added one more to prevent Noel’s sore mouth turning to thrush. He also said ‘lets take a week off, come back to see me in 2 weeks’… So this is also a huge encouragement to us.

This weeks blood tests
White cells 2.9 — Last week 2.4 — Normal 3.8 – 9.2
Red cells 2.89 — Last week 2.76 — Normal 4.2 – 5.6
Platelets 54 — Last week 55 — Normal 155 – 410

Noel did not need any transfusions today so he just got his dressing changed and he also got a ‘flu shot. Which should help protect him from picking up any ‘flu like infections.

In two weeks time when we are back here in Boston it will the same week the Welcome Home Initiative for Veterans of all wars being held at the Spiritual Life Center in Greenwich, NY (12-14th November). Noel is normally a team member and speaker (this would have been his 14th WHI) at this 3 day retreat for veterans and their spouses who are mainly suffering from PTSD and other unseen wounds of war. It is a safe place where they find acceptance, understanding and love and can begin to find healing. Please pray for this retreat and for those who are booked to attend it that they will find the courage to actually attend and while there that the Peace of the Lord will transcend all their nightmares and memories and healing will take place. Please also pray for Noel who is very disappointed he is unable to be there not only because he has to be in Boston but also because he is restricted from meeting with groups of people as his immune system is still not strong.

We both continue to rejoice and be glad as we move forward on this journey. It sometimes seems very long at other times seems to be passing very fast… as we are now just 4 weeks away from Thanksgiving and only 8 weeks away from Christmas!

Please continue to give praise and thanks for all our many blessing and for the Lord’s continuing provision for our needs.

Please continue to pray as other weeks for our family on both sides of the Atlantic and for continuing progress towards restored full health for Noel.

God bless you!

Praise God for His present help in times of trouble. Psalm 46. 1-2.

For I will restore health to you and heal your wounds, says the Lord. Jeremiah 30.17.

We are thanking the Lord for seeing us through difficult times. This past week has seen Noel with slightly more energy and his appetite has been better but his mouth and throat are still very sore and uncomfortable from the GVHD. He doesn’t want to talk much. Thankfully his spirits have been lifted and he felt well enough this week for Deacon Dave to visit on Sunday and bring us the Reserved Sacrament, having missed the last 3 weeks when Noel was not feeling up to having visitors… this was a blessing to us both, and also a visit on Monday afternoon from Bishop Dan encouraged us.

The highlight of this week has been the visit of Noel’s brother Julian, and his wife Ann, from London… they arrived in Boston and drove up to have a late dinner with us on Monday evening before checking into their hotel here in Glens Falls. We spent Tuesday catching up with them. It has been well over a year since we last saw them. We all enjoyed a happy family evening together with Toby, JoAnn and the girls… today Wednesday we left them to explore the local area and Toby once again took the day off work to drive us to Boston and back in the day… We are so grateful to him. Tomorrow, after breakfast with us here at home, Julian and Ann will leave to drive back to Boston for their return flight early Friday morning to London. Seeing his sister and her husband 2 weeks ago and now his brother and his wife has been an enormous blessing and encouragement to Noel.

This week at the Dana-Farber Cancer Institute, Noel saw Amy and she explained how the GVHD, graft verses host disease, is causing some negative ‘activity’ in Noel’s body… evident in his very sore and dry mouth and in his elevated liver function tests, so she doubled his daily dose of steroids… but still assuring us this is a relatively low dose so we need not worry about adverse side effects.

But on the other hand the results of his latest blood DNA/Chimerism test showed it was 95% that of his donor and could be 100% by now. This is such good news and a wonderful answer to prayer, although it brings a higher risk of more GVHD activity especially in his liver… so a very close watch is now being keep on Noel and we return next week for another appointment… There was little change in his other blood levels. Which this week were…

White blood cells 2.4 — Last week 1.8 — Normal is 3.8 – 9.2 — So a slight rise
Red blood cells 2.76 — Last week 2.78 — Normal is 4.2 – 5.6 — Little difference
Platelets 55 — Last week 62 — Normal is 155 – 410 — Just a slight drop

We hope with the increase of steroids Noel will continue to gain more strength and the GVHD will not become any worse or cause any lasting damage but will soon start to show signs of improvement as the donors cells begin to reconsider Noel as being part of them selves.

He continues to have a compromised immune system so is still restricted in his activities.

JoAnn and her sisters, Judy and Melanie left today for a short cruise. They have been planning this little holiday together for over a year… I am trying to help out more with Charlotte and Lucy while JoAnn is away and to also give her parents a bit of a break as her father has not been well recently. They have been doing their and our share of the girls’ day care for almost 5 months now besides still working their own jobs. We have been so grateful that they have been willing to shoulder this extra load – another answered prayer!

Please give thanks with us for…

• the ways our needs are being met.
• the blessings we see daily.
• for good friends and family.

Prayers please along these lines…

• for Noel to regain his strength.
• for his liver not to be damaged by the GVHD.
• for his sore and dry mouth and throat to heal [then he will want to talk again, :-), hmm!]
• for his new bone marrow to make more good blood cells.
• for safe travel to and from Boston each week….especially as the weather is now changing.
• for our family here and in England.
• for Ron, JoAnn’s father that his health problems will soon be sorted out and he will feel better.

We are grateful that you are still reading our updates and for your messages of encouragement here on the internet and in the mail and on the telephone. 🙂

God Bless you.

Hope Lodge, Boston

Thank you all for all your prayers this past week. Last week’s not so encouraging news turned out today to be much more encouraging. Praise the Lord for strengthening Noel and sustaining us through these difficult days!

The Lord will sustain him on his sickbed and restore him from his bed of illness. — Psalm 41.3

Today, Noel was scheduled to see Amy, Dr. Soiffer’s NP, although Dr. S did pop into the consulting room to share the better news with us… Noel’s blood work today showed a slight rise in his red cells and platelets. His liver and kidney functions were much better and the chimerism DNA test showed his donor’s cells to be on the increase again back up to nearly 60%. All very good signs. So although he still has the extremely uncomfortable and debilitating GVHD (graft-verses-host-disease) and is not feeling much better, there are good positive signs things, including the building up of a new immune system and fighting the GVHD, are moving in the right direction. This is all very encouraging and we are so grateful to the Lord for answering all the prayers from around the world… Please keep praying- prayer works!

The steroids seem to be having a good effect, so Noel will remain on them at the same low level and continue to see how he feels. It is better for the long term to be on lower doses as this lessens the likelihood of nasty side effects. His very sore mouth makes eating hard so he is mainly on a diet of soup with soft bread and Ensure (a special over-the-counter health drink). He longs for the day he can go out for a nice prime rib or something Chinese or Indian. Thankfully he has not lost any more weight which is also a good sign.

This weeks blood tests
White cells 1.8 — Last week 2.5 — Normal 3.8 – 9.2 — So a slight drop this week 🙁
Red cells 2.78 — Last week 2.42 — Normal 4.2 – 5.6 — So a slight rise 🙂
Platelets 62 — Last week 34 — Normal 155 – 410 — So a better increase here 🙂

Although the oral steroids Noel is taking are helping him generally feel better, he is still tired and fatigued and needs to rest a lot – but his spirit is encouraged by today’s better news, as is mine. Last week when his sister and brother-in-law were here he only got short ‘at home’ visits with them and felt unable to join me when I took them out and about sightseeing in the local area. But even the short time together was enjoyed by everyone and we are so grateful for them making the effort to fly over from London to visit us.

Next week Noel’s brother and sister-in-law, also from London, fly in for a short 4 day visit and we hope Noel will be feeling much better by then. Unfortunately we do have to be in Boston again next Wednesday for more blood work and a review appointment. But we are hoping Toby might be able to be our driver again and we can do it all in the day like last week, so as to maximize the time with Julian and Ann. Charlotte is looking forward to seeing them and they will be meeting Lucy for the first time.

The past 2 Sunday’s we have missed receiving the Reserved Sacrament as Noel has not felt well enough for Deacon Dave to come over for a visit; but hopefully this next week things will be different.

Last week our son Charles was in California and, this week, Florida for his work. Both on the same continent as we are but too far away to visit… He, Sarah, Eve and Will are all well and doing great. So are Toby, JoAnn, Charlotte and Lucy.

Please pray this week for:

• the donor cells to grow and multiply in Noel’s bone marrow.
• for all his blood tests to be moving towards being normal.
• for increased energy and vitality.
• for the GVHD to subside and his sore mouth and other side effects to get better.
• for our plans to travel to Boston next Wednesday, October 24th.
• for Julian and Ann to have safe travel and a good stay in the USA.

We are sorry we have not been better at returning your calls and reply to your messages but even as it is far from normal, life seems more than normally busy. Noel especially has not felt up to either speaking on the phone much or dealing with email etc. But please don’t stop calling or writing as you encourage us so much. God bless you!

I will lift up my eyes to the Hills, from where comes my help. My help comes from the Lord, who made Heaven and Earth… AMEN! — Psalm. 121. 1-2

Glens Falls, Thursday 11th October 2012

This is the day the Lord has made ; let us rejoice and be glad in it. Psalm 118:24

The joy of the Lord is our strength. Nehemiah 8:10

Therefore we do not lose heart. Though outwardly we are wasting away, yet inwardly we are being renewed day by day… So we will fix our eyes on not what is seen but what is unseen, for what is seen is temporary, what is unseen is eternal. 2 Corinthians 4.16-18

This weeks news is not so encouraging as we would have hoped for. Noel has not felt well for nearly 13 days now, since before we returned, returning home from our extra visit to Boston last Thursday. He even asked me to drive all the way home as he just did not feel up to it. He then spent most of the last 6 days feeling very under the weather, resting and sleeping.

This week our son Toby offered to take time off work so he could drive us to Boston for Noel’s appointments, there and back in the day (something I could not do; and Noel could not have done this week and would not normally do unless no other solution were available). This was a huge blessing as it meant we could spend more time with Noel’s sister and brother in law who are visiting this week from England, staying in a local hotel.

After a phone call on Tuesday with Amy, Dr. Soiffer’s NP we had thought that there was a chance Noel would be admitted to hospital and she suggested that we pack overnight bags just to be on the safe side, we are very grateful he was not kept in Boston, for many reasons!

Noel saw Dr. Soiffer yesterday and on hearing how Noel felt and reviewing his blood results confirmed that the ‘activity’ Noel is experiencing is mild GVHD, Graft-verses-Host Disease. This is actually considered, at this stage 100 plus days after a stem cell transplant, not to be uncommon and is known as Chronic GVHD (before the 100 day point it is known as Acute).

Graft-verses-Host Disease is when the donors white cells (known as ‘T’ cells) become very active and begin to grow and identify the patients organs and body tissues as ‘non-self’ attacking them and reducing their ability to work normally.

Noel will continue to take the the immunosuppressive drugs he has been on since his transplant and Dr. Soiffer has started him on a course of steroids. This should help Noel to feel much better in a few days.

Noel’s blood test results this week showed little change and he did need to have a unit of red blood cells and a liter of hydration fluids by infusion but his platelet count was up so he did not need to receive any platelets. His levels all still remain lower than they should be.

Blood test results:
Red cells 2.42 – Last week 2.52 – Normal 4.2-5.6
White cells 2.5 – Last week 3.7 – Normal 3.8-9.2
Platelets 34 – Last week 19 – Normal 155-410

Dr. Soiffer is concerned but not worried and will continue to keep a close eye on Noel saying he will see him weekly, This, of course, is a little disappointing as we had been so looking forward to not having to make the long journey to Boston every week.

It has been good having Joycelin and Bill here. But sad they have not had the quality time with Noel we had all hoped for. But they have been able to do some local sight seeing and we did have a family meal with Toby, JoAnn and Charlotte, whom they last saw in Ireland at a family wedding in 2009, and they met Lucy for the first time.

Prayers please for:

• Noel to feel better, less fatigued, less cold, for his digestive system to return to normal and his sore mouth and throat to heal. Noel says if this is how one feels with mild GVHD he cannot begin to imagine what a full blown dose would feel like.
• For the steroids to be effective with no lasting side effects.
• For safe travel weekly to and from Boston.
• For us to keep our focus on the Lord and all his many blessings.
• For our family here and in the UK.

Thank you for your prayers, love and support during this difficult time.

God bless you.

Happy Meryl on a sunny afternoon at Crandall Park, Glens Falls, New York
September 1, 2012

D+107:September 26, 2012– And Feeling Good, Praise God!

Doxology: Revelation 5:13 (Louis Bourgeois and Thomas Ken)

Praise God, from Whom all blessings flow;
Praise Him, all creatures here below;
Praise Him above, ye heav’nly host;
Praise Father, Son, and Holy Ghost.
Amen.

Thank you all so much for your messages and ‘likes’ on this site, and at CaringBridge and Facebook (Click the links on the home page to access them), let alone your prayers and good wishes. Thanks for all the cards, letters, phone calls and a few home visits too. We welcome every one of them.

Today is the first Wednesday in nearly 4 months we have not had to see my specialist in Boston. I didn’t realize what a pleasant relaxation not having to be there would be! Although my energy levels are not yet what they need to be, being at home gives me an incentive to get on and do some of the things that have dropped by the wayside recently, especially answering emails and social media messages, as well as praying for God’s overwhelming blessings on each person replying to these ‘posts’.

Health condition seems unchanged since last week, so we pray this good news continues and is reflected in better blood counts in Boston next Wednesday.

I bought a bike recently and have gone out on it a couple of times as part of my campaign to get fit again. I cycled 5 miles on a local cycle path (largely flat) last Friday and by the time I got home my legs were like jelly! I didn’t realize this illness would cause me to be so out of condition. Once the Hickman line (a port) is taken out of my chest – maybe next week – and the wound heals up, and the doctor gives me permission to do so, I’m looking forward to doing some gentle swimming at our local YMCA swimming pool, if I can find a quiet time to go. However, with the Autumn/Winter flu season soon to start, I suspect this might not happen for quite a while. 🙁

Didn’t get to sail my small dinghy this year either. 🙁

Following on from Meryl’s comment about an impromptu support group of combat Veterans and Bone Marrow transplantees at Dana-Farber Cancer Institute (DFCI) last week, I’m asking each of you to pray for the upcoming Welcome Home Initiative (WHI) Retreat – the 14th one, 12th at the Greenwich, NY Christ the King Spiritual Life Center. It takes place from November 12-14. There are about 30 combat Veterans, several spouses and the largest number of female Veterans coming we have ever welcomed. I want to carry out my usual role of co-leader, leading the two Tuesday morning sessions, but it looks extremely unlikely at this stage. So pray for a miracle to happen that the doctor says I can be involved. Also pray for the right number and quality of hosts to be available for every Veteran. Pray for sufficient money to run the Retreat, which is free for the Vets. See www.christ-the-king-center.org/WelcomeHome for more details. How about a STAFFORD Vet coming sometime? (I served and did my combat tours in Northern Ireland with the STAFFORDS – The Staffordshire Regiment). 🙂

Pray also for a highly successful Warrior Retreat taking place near Fort Campbell, Kentucky, from October 4-6. This has been inspired by the example of the WHI Retreats. I was asked to help but I had to tell the pastor organizing it yesterday that I am not able to go. Fort Campbell is a key base for Special Forces and the 101st Airborne Division (Air Assault). The STAFFORDS and 101st have a historical connection. The 101st jumped into Nijmegen, Holland as the South Staffords landed by glider near Oosterbeek, to the west of Arnhem. The STAFFORDS and its successor regiment, 3 MERCIAN (STAFFORDS) commemorate the Arnhem battle on September 17 annually. 🙂

Finally today, I want to pay a very special tribute to my wonderful wife, caregiver extraordinaire and Special Angel. She’s a Special Angel ’cause no other woman would ever put up with the likes of me for the 44 years we have known each other. She is the most unconditionally loving person I have ever known and she is always here for me. Thank you, Meggiewife (and I’m the only person who ever uses that name)! 🙂

Hope Lodge, Wednesday 19th September 2021

Jesus spoke to them, saying, “Be of good cheer!”.
Mathew 14:27.

“For I know the plans I have for you” declares the Lord “not to harm you, plans to give you hope and a future”.
Jeremiah 29:11

Today is a ‘special’ day and one of good cheer! 100 days since Noel received the gift of new life in the form of stem cells from an unrelated donor. Donors are special people as they freely volunteer and receive nothing in return except the grateful thanks of those who receive their gift. We thank God for them and all the many doctors, nurses and other patients that over the years have made stem cell transplants one of the Lord’s miracles here on earth.

+ 100 days…. What does is actually mean? For Noel, it means he is very blessed and has survived the most dangerous initial post transplant period, when some people do suffer very difficult physical symptoms including rejection of cells, Graft Verses Host Disease (GVHD) and even death. Noel experienced some difficulties over the past weeks but one’s that were in hindsight short lived and although serious and unpleasant passed without long-lasting consequences. At the 100 day point for many the significant change would be being able to return home. We have met many patients who after their Stem Cell transplant have had to remain close to the hospital for 100 days but Noel was blessed in the fact that his doctor was willing to let him leave after a month and return each week for a visit since he was doing well and we live close enough (225 miles each way) from Boston, to make this feasible… Thank you Lord!

At this stage his doctor would normally begin reducing many of the post transplant drugs but this already has been steadily happening over the last few weeks as some of Noel’s drug doses have been reduced to prevent increasing toxicity in his kidneys and liver… We saw Amy, Dr. Soiffer’s NP, today and she said both Dr. Soiffer and she were pleased with Noel ‘s progress at this stage… and although his blood levels are still remaining low they are pleased he reports feeling well.

On seeing his low blood numbers today she did offer him red cells but we all agreed that as he was not feeling unwell and, himself, did not feel he needed them, she would be happy for him not to have them but to see what the progress is over the next couple of weeks – so Noel chose to wait. Too many transfusions of red cells can cause dangerous problems with iron overload in the blood.

Noel had hoped today to have his Hickman line removed but as his platelets were low, Amy said the medical team would require him to have a unit of platelets by transfusion before they removed it to prevent any excess bleeding during the procedure. Amy and Noel made the decision not to remove it today but to wait until his platelets are higher. So we continue with the nightly routine of flushing his lines at home, as well as protecting the dressing before he showers by waterproofing it with a plastic covering.

Today’s blood count results… not a great change… stable but too low!
Red cells 2.83 — Last week 2.93 — Normal 4.2 – 5.6
White cells 2.5 — Last week 2.3 — Normal 3.8 – 9.2
Platelets 29 — Last week 37 — Normal 155 – 410

Praise the Lord for other progress signs today! Noel is moving towards fortnightly visits to see Dr. Soiffer or Amy. They said Noel can skip next week and return on October 3rd for his next appointment. But if he is feeling unwell at any time he must call them.

Some of Noel’s dietary restrictions have also been lifted… Noel can now eat some ‘take out’ restaurant food but this has to be freshly and well cooked. No food that has been sitting around under the heat lamps! We are not great ‘take out’ food eaters but it is good to know that he is progressing and getting back to normal. He cannot yet eat in a restaurant as he is still on restrictions of being with the public in public places. The restriction of uncooked fresh vegetables and salad is also lifted but only for items washed at home… No ‘take out’ salad bars or pre-packed salads.

Amy said the Fall and Winter cold and flu season will most likely lengthen the time Noel has the restrictions on him of being with the public in public places… like social meetings, crowded shops, Church and travel. Although this is somewhat frustrating we will be very cautious and follow the rules. To risk getting sick is just not worth it for either of us, a few missed meetings etc. is nothing when we think of the extra years to participate in everything this process will give us.

Last weekend was blessed again by receiving the Reserved Sacrament from Deacon Dave on Sunday afternoon. On Monday we had a fun ‘tea time’ with our good friends Jeph and Barbara from Lake George. Their motel season is almost over so they are able to relax a little and spend time away from the job… we first met them just about 5 years ago… a chance meeting in a local coffee shop and have been good friends ever since.

You never know what plans the Lord has for you in chance meetings! Today we sat down in the waiting area at the Dana Farber and found ourselves with a very highly decorated (for valour) US Marine Viet Nam Veteran; and the parents of a serving Marine who is also married to a Marine, both with tours in both Iraq and Afghanistan. Both these men had had stem cell transplants so we were able to talk to them about shared experiences and Noel shared with them about the work he does with the Welcome Home Initiative Retreats in which they both showed interest. We were able to pray briefly with them, as well as with several others during this visit to Boston.

Being the 100th day we also decided to revisit the Brigham and Women’s Hospital ward and say hello and thank you to the transplant unit nurses… Those on duty were very encouraged to see us and see Noel looking so well. They promised to pass on our greetings to the rest of the team.

Prayer requests are on the same lines as before:

• For Noel to continue to feel well, to have increased energy, for his blood counts to improve.
• For our family in both the UK and USA to all be well as life is busy with work and school for them all.
• For us both to remain healthy and free from seasonal bugs.
• For continued safe travel as we enter in to the variations of the seasonal weather.
• Noel is approaching his many military contacts to find a suitable speaker for the Closing Ceremony of the next Welcome Home Initiative (WHI) on November 14. So far several have been invited to speak but none are able to do so. Noel is not expecting to take part in this retreat, although he dearly wants to. Pray for the Lord to “provide” the right speaker.

Praise the Lord with us for all his many blessings, for the plans he has for us and for his continuing provision for us. We also praise and thank Him for all of you, near and far who faithfully stick with us and encourage us and support us… You are such a blessing, thank you.

God Bless you and your loved ones!

*** Unless there is anything to report in the meantime my next update will be written after Noel’s appointment here in Boston on October 3rd. 2012. ***

Written in Boston, Wednesday 12th September 2012.

“Then our mouth was filled with laughter and our tongue with singing……The Lord has done great things for us and we are glad.”. Psalm 126: 2-3

“A merry heart does good, like medicine… ” Proverbs 17: 22

Over a year ago when Noel was first taken ill and diagnosed with cancer we both decided that we would trust in the Lord our God to have a plan for our good, we would not be downhearted or allow anything to rob us of our joy. So we praise the Lord that we have been able to keep our focus on the positive and have been able to remain cheerful and our lives have been filled with much joy and laughter… some people may find us a little strange but hopefully they find us encouraging too.

From one week to the next time seems to go increasingly fast and this week sees Noel at +93 days since his transplant. Back in June, day +100 seemed so far away but now it is just one week away… For us it will bring two changes… After next week Noel moves on to fortnightly appointments at the Dana Farber Cancer Institute, so long as nothing unusual suddenly happens with his progress. And he will have the Hickman Line removed… he will be glad not to have to stick on a waterproof cover every time he takes a shower and for me to not have to flush out his access lines each night. Although no longer having it will mean at each appointment he will have to have an IV put into his arm so they can draw the 9 to 13 vials of blood they use for his tests and if needed to receive blood products through, although this will be removed after each appointment.

Transplant Day plus 93 September 12, 2012

This week Noel saw Dr Soiffer and he had a Harvard medical student with him as the Dana Faber is also a teaching hospital. Dr Soiffer said it is still early days in this long recovery process, Noel’s blood test results this week show little change from last week, just very slightly lower but Noel feels well and looks good so Dr S. is not too concerned.

Dr S. looked at Noel’s right foot as last Friday Noel had called him because his foot was suddenly and inexplicably extremely painful. Dr S. said he thought it was gout (!) and that Noel should see his Primary Care doctor, which he did on Friday afternoon; he also thought it was gout… prescribed pain killers and suggested Noel went back to drinking the 3 liters of water a day. Thankfully his foot is now looking much better and the pain has gone.

This weeks Blood test results. Still low but Praise the Lord… relativity stable.

Red Blood cells 2.93 — Last week 3.12 — Normal 4.2 – 5.6
White Blood cells 2.3 — Last week 2.5 — Normal 3.8 – 9.2
Platelets 37 — Last week 38 — Normal 155 – 410

You may remember I wrote about a DNA test called a Chimerism. When I said Noel’s DNA was 14% his own and 86% his donors… Noel and I had misunderstood the result that was being sought… We thought we were waiting to see the DNA being 100% Noel’s but what we are actually waiting to see is for Noel’s blood DNA to be 100% that of his donor! This seems a little strange but since the blood manufacturing stem cells in Noel’s bone marrow are those that were transplanted from the donor it actually makes sense. At this stage some transplant patients blood changes and becomes the same blood type as their donor but Noel was fortunate as his donor was A Positive, the same as he is.

We are so blessed to be able to stay here at the American Cancer Society’s AstraZeneca Hope Lodge… Accommodation is offered here to cancer patients and their care givers free of charge no matter if your stay is for several months or just a few days… funding for this is provided through fund raising and donations to the American Cancer Society and by the drug company AstraZeneca. This evening we had a group of research scientists from the company come to give us a presentation about their work in developing new cancer drugs… which was most interesting. They also brought a light supper of sandwiches and cookies for us all to enjoy (except for the transplant patients, including Noel, who sadly cannot have outside food: Noel cast his eyes longingly over the delicious ham, cheese and salad rolls!)

Family news is all good. Our granddaughters Charlotte and Eve both took big school in their stride and seem to be doing great. And everybody else is doing well… and keeping very busy.

Although the daytimes here in the Northeast are still very warm the nights are definitely getting cooler and Fall (Autumn) is on the way… we are looking forward to the changing colors of the leaves as we drive to and from Boston… the New England area is famous for the beautiful foliage at this time of the year.

We have continued to be blessed this past week by your support, cards, messages and telephone calls of encouragement along with a visit from our good friend Michael, the first English man we met in Glens Falls five years ago, and a visit from Deacon Dave and his wife Barbara, who shared the blessing of the Reserved Sacrament with us. We are not sure when we will be allowed by the Doctor to attend Church again… Noel’s blood counts need to be higher before he can be with groups of people again. I could of course attend Church but have decided to avoid being around people as much as possible as if I was to catch even just a slight infection it could be very serious for Noel if I passed it on to him…

Please continue to pray along the same lines as other weeks, travel safety, rise in blood counts and general well being for us both and give the Lord all the Glory for answered prayers and His provision for our needs.

You are all in our prayers, God Bless you and your loved ones.