Re: Cancer and SCD - UPDATE

[Guest guest]

we're all praying -hang in - can they IV the meds instead of giving them

orally??? just a thought??? healing is coming -congrats on the trophies and i'm

sure they'll be back, and you'll be healthier than ever!!

Hugs!!!! God Bless!!!

Eileen 19 months scd

>

> Hi Gitte, Thank you for the update – I was wondering how you were doing. It

> sounds like good news although I am sure it must be hell to go through.

> Perhaps once the cancer treatment is finished, your gut can finally heal! I

> hope so. Hang in there and please keep us updated as to your progress. We

> are all rooting for you!

>

> Carol

>

> CD 21 yrs SCD 4.5 yrs

>

>

>

> From: BTVC-SCD [mailto:BTVC-SCD ] On Behalf

> Of gittealbertsen

>

> A short update on my cancer story so far: I had one breast removed and will

> start chemo on Friday. Then radiation and hormone suppresants. So there's a

> long way home, but it made it a lot easier to cope, when I got some great

> news after the operation: They removed one of my breasts completely and a

> lot of the lympho(?) in the arm pit, but it appeared to be smaller and less

> aggressive than first expected and had only spread to one of those

> lymphos(?)!

>

> So I have much better odds to work with now. I give the full credit for this

> to the healer, I have been working with intensely since I was diagnosed. The

> hospital doesn't understand what happened and can't explain it - but are, of

> course, not willing to hear about healing or anything else. Just think about

> all the experiences and good ideas, they are missing out on!

>

> The weird thing is, that the SCD works a lot better again. Until last X-mas

> I was slowly but constantly healing and then it went all down hill. I have

> done nothing but eliminating from the diet and gone back to intro several

> times. Nothing really helped. But since my surgery, where they removed the

> cancer, my stomach is healing again. I just had trophies for the first time

> in 8 months! Yee-ha! :-) It's like my body was too busy trying to cope with

> more important things. Now it can concentrate on my Crohn's.

>

> I'm now a bit nervous of what will happen, when I start chemo on Friday.

> Apart from loosing my hair, getting nauseaus etc., it might also effect my

> Crohn's. Also it is very hard to convince the doctors here, that I can not

> have any medication taken orally. And we can't have things compounded

> according to Danish legislation. I will hate to comprimise on that but I

> will probably have to.......

>

> Thanks for listening :-)

> Gitte from Denmark

> Crohn's 30 y

> SCD 2½ y

>